Autosomal dominant dilated cardiomyopathy
[DOC File]Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
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A familial history of ARVC is present in 30% to 50% of cases, and the disease is considered a genetic cardiomyopathy, usually inherited in an autosomal dominant pattern with variable penetrance and expressivity; in addition, autosomal recessive forms have …
[DOCX File]GeneDx
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Dilated cardiomyopathy mostly is a disease of large and giant breeds, but it also strikes certain breeds at a much higher rate than other breeds of the same size. ... Some preliminary evidence consistent with an autosomal dominant mode of inheritance (in which the presence of only one gene for DCM is needed for the disease to develop) has been ...
[DOC File]CARDIOMYOPATHY
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Autosomal dominant transmission means that a single copy of the abnormal gene is sufficient to cause the disease. On the other hand, a person with the abnormal gene will not necessarily develop any features of the disease. ... Dilated cardiomyopathy: This will result in increasing symptoms of heart failure. 3. Ventricular aneurysms: These may ...
Dilated cardiomyopathy | Genetic and Rare Diseases Information C…
Dilated cardiomyopathy can be inherited in an autosomal dominant, autosomal recessive, X-linked, or mitochondrial manner. Multiple national and international medical societies have published guidelines that recommend genetic testing for DCM and other cardiomyopathies:
[DOC File]Dilated Cardiomyopathy: - CANIS MAXIMUS
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Dilated cardiomyopathy is usually inherited in an autosomal dominant manner. However, autosomal recessive, X-linked and mitochondrial inheritance pattern has also been observed. In cases of mitochondrial inheritance, it becomes critical to test if mother carries a mutation because mitochondrial mutations have 100% chance of inheritance from ...
[DOC File]Microsoft
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In these age groups, deaths due to cardiomyopathies (including arrhythmogenic, dilated, hypertrophic and restrictive) are the leading cause of SCD.1,3 Of the cardiomyopathies, hypertrophic cardiomyopathy (HCM) is the form most notorious for causing SCD, often in young, otherwise healthy, athletes.3 While HCM is a well-known clinicopathologic ...
[DOC File]Date:
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Dilated cardiomyopathy. Hypertrophic cardiomyopathy. Restrictive cardiomyopathy. Secondary cardiomyopathy (secondary involvement of the myocardium due to a systemic disease) Inflammatory: ... (autosomal-dominant defect) was established in 50% to 60% of cases. The latest reports, based on extensive and detailed genetic studies confirmed the ...
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